Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3012263937

FEI Number

3012263937

Entity Name

WENZHOU SENDE DIANZI SHANGWU CO., LTD

City/State/Country

Wenzhou Zhejiang, CN

Establishment Address

1813 Chengyuan Building, 5052 Airport Avenue, Luncheng District, Wenzhou Zhejiang 325000, CN

Establishment Type(s)

Export Device to the United States But Perform No Other Operation on Device,Foreign Private Label Distributor,Manufacture Medical Device

Owner / Operator

Wenzhou Sende Dianzi Shangwu Co., Ltd (Owner Number: 10051584)

Owner / Operator Contact Address

1813 Chengyuan Building, 5052 Airport Avenue, Luncheng District, Wenzhou, CN-ZJ 325000, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HOI	Spectacle, Magnifying	Ophthalmic	Class 1	886.5840	2016-04-07

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar Corp Email: david.lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

Wenzhou Sende Dianzi Shangwu Co., Ltd

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3012263937. Last updated year: 2026. Please use registration number 3012263937 when referencing this establishment in official correspondence.